Gene: POLG ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathy. 22342071 2012
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Early-onset ataxia with progressive external ophthalmoplegia associated with POLG mutation: autosomal recessive mitochondrial ataxic syndrome or SANDO? 22931735 2012
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR MELAS/SANDO overlap syndrome associated with POLG1 mutations. 21647632 2012
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts. 21138766 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Molecular and biochemical characterisation of a novel mutation in POLG associated with Alpers syndrome. 21235791 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Novel POLG splice site mutation and optic atrophy. 21670405 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Parieto-occipital lobe epilepsy caused by a POLG1 compound heterozygous A467T/W748S genotype. 21515089 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Stroke and Stroke-Like Symptoms in Patients with Mutations in the POLG1 Gene. 23430834 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Bowel obstruction in patients with Alpers-Huttenlocher syndrome. 22006280 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic study. 19538466 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Sensory ataxic neuropathy with dysarthria/dysphagia and ophthalmoplegia (SANDO). Two case reports. 22616202 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Mitochondrial DNA polymerase gamma mutations: an ever expanding molecular and clinical spectrum. 21880868 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR POLG exon 22 skipping induced by different mechanisms in two unrelated cases of Alpers syndrome. 20691285 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 GeneticVariation phenotype CLINVAR Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing. 20843780 2011
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Sensory ataxic neuropathy with dysarthria and ophthalmoparesis (SANDO) in late life due to compound heterozygous POLG mutations. 20513108 2010
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO) in a sibling pair with a homozygous p.A467T POLG mutation. 19813183 2010
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR POLG1 variations presenting as multiple sclerosis. 20837861 2010
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR To review our clinical experience and determine if there are appropriate signs and symptoms to consider POLG sequencing prior to valproic acid (VPA) dosing in patients with seizures. 20138553 2010
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Cerebral folate deficiency and CNS inflammatory markers in Alpers disease. 19766516 2010
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR [Mitochondrial DNA depletion and POLG mutations in a patient with sensory ataxia, dysarthria and ophthalmoplegia]. 20576279 2010
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 GeneticVariation phenotype CLINVAR POLG, but not PEO1, is a frequent cause of cerebellar ataxia in Central Europe. 20803511 2010
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 GeneticVariation phenotype CLINVAR mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae. 20185557 2010
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. 20818383 2010
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 CausalMutation phenotype CLINVAR Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase γ (POLG1). 21686371 2009
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.430 GeneticVariation phenotype CLINVAR Ataxia with ophthalmoplegia or sensory neuropathy is frequently caused by POLG mutations. 19752458 2009